1,5-Cyclooctadiene, 3-(1-methyl-2-propenyl)-

Details

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Internal ID 9c6edaa5-7244-4488-b166-501bf1863227
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Cyclic olefins > Cycloalkenes
IUPAC Name (1Z,5Z)-3-but-3-en-2-ylcycloocta-1,5-diene
SMILES (Canonical) CC(C=C)C1CC=CCCC=C1
SMILES (Isomeric) CC(C=C)C/1C/C=C\CC/C=C1
InChI InChI=1S/C12H18/c1-3-11(2)12-9-7-5-4-6-8-10-12/h3,5,7-8,10-12H,1,4,6,9H2,2H3/b7-5-,10-8-
InChI Key XDAVQTXWOCTEPO-RRMOSLQNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18
Molecular Weight 162.27 g/mol
Exact Mass 162.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.72
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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1,5-Cyclooctadiene, 3-(1-methyl-2-propenyl)-
3-(1-Methyl-2-propenyl)-1,5-cyclooctadiene #

2D Structure

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2D Structure of 1,5-Cyclooctadiene, 3-(1-methyl-2-propenyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.8867 88.67%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.6620 66.20%
OATP2B1 inhibitior - 0.8641 86.41%
OATP1B1 inhibitior + 0.9450 94.50%
OATP1B3 inhibitior + 0.9595 95.95%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9288 92.88%
P-glycoprotein inhibitior - 0.9763 97.63%
P-glycoprotein substrate - 0.9329 93.29%
CYP3A4 substrate - 0.6340 63.40%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.7561 75.61%
CYP3A4 inhibition - 0.9709 97.09%
CYP2C9 inhibition - 0.9241 92.41%
CYP2C19 inhibition - 0.8997 89.97%
CYP2D6 inhibition - 0.9562 95.62%
CYP1A2 inhibition - 0.6875 68.75%
CYP2C8 inhibition - 0.9664 96.64%
CYP inhibitory promiscuity - 0.8179 81.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.5072 50.72%
Eye corrosion + 0.9835 98.35%
Eye irritation + 0.9567 95.67%
Skin irritation + 0.7354 73.54%
Skin corrosion - 0.8967 89.67%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4874 48.74%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.8818 88.18%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6077 60.77%
Acute Oral Toxicity (c) III 0.7857 78.57%
Estrogen receptor binding - 0.9276 92.76%
Androgen receptor binding - 0.9121 91.21%
Thyroid receptor binding - 0.8222 82.22%
Glucocorticoid receptor binding - 0.6601 66.01%
Aromatase binding - 0.8968 89.68%
PPAR gamma - 0.8180 81.80%
Honey bee toxicity - 0.6392 63.92%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9843 98.43%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.65% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.44% 97.25%
CHEMBL2581 P07339 Cathepsin D 81.33% 98.95%
CHEMBL3055 P50613 Cyclin-dependent kinase 7 80.78% 81.88%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.66% 96.47%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.49% 90.24%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 5367436
NPASS NPC216519